大理大学学报 ›› 2021, Vol. 6 ›› Issue (2): 46-50.DOI: 10. 3969 / j. issn. 2096-2266. 2021. 02. 009

• 药学 • 上一篇    下一篇

基于网络药理学预测痛泻要方治疗炎症性肠病的作用机制

索光喜,胡倘潇,肖天保*   

  1. (贵州中医药大学研究生院,贵阳550000)
  • 收稿日期:2020-06-06 修回日期:2020-08-26 出版日期:2021-02-15 发布日期:2021-03-17
  • 通讯作者: 肖天宝,主任医师,E-mail:402020134@qq.com。
  • 作者简介:索光喜,硕士研究生,主要从事中医诊治肛肠疾病研究。

The Mechanism of Tongxie-Yaofang in Treating Inflammatory Bowel Disease Based on#br# Network Pharmacology

Suo Guangxi, Hu Changxiao, Xiao Tianbao*   

  1. (Graduate School, Guizhou University of Traditional Chinese Medicine, Guiyang 550000, China)
  • Received:2020-06-06 Revised:2020-08-26 Online:2021-02-15 Published:2021-03-17

摘要: 目的:利用网络药理学探讨痛泻要方治疗炎症性肠病的作用机制。方法:借助TCMSP数据库检索痛泻要方的有效化学
成分和作用靶点,通过GeneCards、OMIM数据库检索疾病靶点,使用R语言筛选出共有靶点,利用Cytoscape软件构建“药物成
分-疾病靶点”网络,通过STRING网站构建共有靶点蛋白互作网络,筛选出核心靶点并进行GO功能分析和KEGG通路富集分
析。结果:共筛选出39 个有效药物成分和125 个成分靶点,其中成分与疾病的共有靶点104 个,核心靶点为IL6、AKT1、
MAPK3、JUN、CASP3、MAPK1等,GO分析涉及的分子功能主要为氨基结合、核受体活性、转录因子活性、磷酸酶结合、类固醇激
素受体活性等。KEGG通路富集分析主要为肿瘤坏死因子信号通路、IL-17信号通路、Toll样受体信号通路等。结论:痛泻要方
通过“多成分-多靶点-多通路”治疗炎症性肠病,为下一步进行实验验证及新药研发提供参考。

关键词: 痛泻要方, 网络药理, 炎症性肠病, 靶点, 作用机制

Abstract: Objective: To study the mechanism of Tongxie-Yaofang in treating inflammatory bowel disease using network pharmacology.
Methods: Effective chemical compositions and targets of drugs in Tongxie-Yaofang was searched in the Traditional Chinese Medicine
System Pharmacology Database and Analysis Platform(TCMSP). Then the targets of IBD were obtained through GeneCards and
OMIM databases, the R software was used to find the common target and a "pharmaceutical component-disease target" network was
constructed by means of Cytoscape software. Finally, a common target protein interaction network was constructed through the STRING
website, core targets were screened out and the mechanism of its action was explored through GO analysis and KEGG pathway
enrichment analysis. Results: The study has found 39 effective pharmaceutical ingredients and 125 biological targets. Among the 104
targets that coincide with the disease, the core targets are IL6, AKT1, MAPK3, JUN, CASP3, and MAPK1, etc. The molecular functions
involved in GO analysis are mainly amide binding, nuclear receptor activity, transcription factor activity, phosphatase binding, and
steroid hormone receptor activity. KEGG pathway enrichment analysis is mainly for TNF signaling pathway, IL-17 signaling pathway,
Toll-like receptor signaling pathway etc. Conclusion: Tongxie-Yaofang is used to treat inflammatory bowel disease through "multicomponents,
multi-targets, and multi-pathways", which lays a foundation for the next step of experimental verification and new drug
development.

Key words: Tongxie-Yaofang, network pharmacology, inflammatory bowel disease, target, mechanism

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